26 articles for thisTarget
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Conformationally Defined Rexinoids and Their Efficacy in the Prevention of Mammary Cancers.
University of Alabama At Birmingham
Potent inhibition of human sulfotransferase 1A1 by 17a-ethinylestradiol: role of 3'-phosphoadenosine 5'-phosphosulfate binding and structural rearrangements in regulating inhibition and activity.
University of Alabama At Birmingham
Methyl substitution of a rexinoid agonist improves potency and reveals site of lipid toxicity.
University of Alabama At Birmingham
Methyl-substituted conformationally constrained rexinoid agonists for the retinoid X receptors demonstrate improved efficacy for cancer therapy and prevention.
University of Alabama At Birmingham
Pyrrolidinobenzoic acid inhibitors of influenza virus neuraminidase: the hydrophobic side chain influences type A subtype selectivity.
University of Alabama At Birmingham
Identification of novel inhibitors of bacterial surface enzyme Staphylococcus aureus Sortase A.
University of Alabama At Birmingham
Tethered dimers as NAD synthetase inhibitors with antibacterial activity.
University of Alabama At Birmingham
3-Amino-5,5-dimethylhexanoic acid. Synthesis, resolution, and effects on carnitine acyltransferases.
University of Alabama At Birmingham
Virtual screening to identify lead inhibitors for bacterial NAD synthetase (NADs).
University of Alabama At Birmingham
Synthesis and Structure-Activity Relationships of 5'-Aryl-14-alkoxypyridomorphinans: Identification of a μ Opioid Receptor Agonist/δ Opioid Receptor Antagonist Ligand with Systemic Antinociceptive Activity and Diminished Opioid Side Effects.
University of Alabama At Birmingham
Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent.
University of Alabama At Birmingham
Conformationally defined retinoic acid analogues. 4. Potential new agents for acute promyelocytic and juvenile myelomonocytic leukemias.
University of Alabama At Birmingham
Conformationally defined 6-s-trans-retinoic acid analogs. 3. Structure-activity relationships for nuclear receptor binding, transcriptional activity, and cancer chemopreventive activity.
University of Alabama At Birmingham
A conformationally defined 6-s-trans-retinoic acid isomer: synthesis, chemopreventive activity, and toxicity.
University of Alabama At Birmingham
Conformationally defined 6-s-trans-retinoic acid analogs. 2. Selective agonists for nuclear receptor binding and transcriptional activity.
University of Alabama At Birmingham
Comparative molecular field analysis of hydantoin binding to the neuronal voltage-dependent sodium channel.
University of Alabama At Birmingham
Effects of log P and phenyl ring conformation on the binding of 5-phenylhydantoins to the voltage-dependent sodium channel.
University of Alabama At Birmingham
Bicyclic hydantoins with a bridgehead nitrogen. Comparison of anticonvulsant activities with binding to the neuronal voltage-dependent sodium channel.
University of Alabama At Birmingham
